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FDA 510(k)

IMPROVED TRANSGROW

K-Number: K770876 · 1977-06-03

ApplicantGranite Diagnostics, Inc.
Decision Date1977-06-03
Product CodeJTY
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

IMPROVED TRANSGROW is the device name listed in this FDA 510(k) record. The listed applicant is Granite Diagnostics, Inc.. It received FDA 510(k) clearance on 1977-06-03 under 510(k) number K770876. The device is classified under product code JTY. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the IMPROVED TRANSGROW?

IMPROVED TRANSGROW is a medical device that received FDA 510(k) clearance on 1977-06-03. The listed applicant is Granite Diagnostics, Inc.. The 510(k) number is K770876.

When did IMPROVED TRANSGROW receive FDA 510(k) clearance?

IMPROVED TRANSGROW received FDA 510(k) clearance on 1977-06-03, under 510(k) number K770876.

Who is the listed applicant for IMPROVED TRANSGROW?

The FDA 510(k) record lists Granite Diagnostics, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for IMPROVED TRANSGROW?

The FDA product code for IMPROVED TRANSGROW is JTY.

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Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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